Additive Manufacturing Under Lunar Gravity and Microgravity von Reitz, B., Lotz, C., Gerdes, N., Linke, S., Olsen, E., Pflieger, K., Sohrt, S., Ernst, M., Taschner, P., Neumann, J., Stoll, E., Overmeyer, L.

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Mutations in SDHD, A Mitochondrial Complex II Gene, in Hereditary Paraganglioma von Baysal, Bora E., Ferrell, Robert E., Willett-Brozick, Joan E., Lawrence, Elizabeth C., Myssiorek, David, Bosch, Anne, van der Mey, Andel, Peter E. M. Taschner, Rubinstein, Wendy S., Myers, Eugene N., Richard, Charles W., Cornelisse, Cees J., Devilee, Peter, Devlin, B.

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SDHD mutations in head and neck paragangliomas result in destabilization of complex II in the mitochondrial respiratory chain with loss of enzymatic activity and abnormal mitochond... von Douwes Dekker, PB, Hogendoorn, PCW, Kuipers-Dijkshoorn, N, Prins, FA, van Duinen, SG, Taschner, PEM, van der Mey, AGL, Cornelisse, CJ

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Adopt a Bacterium: a professional development opportunity for teacher assistants von Taschner, N P, de Almeida, L G, Pose, R A, Ferreira, R C C

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Spectrum of Mutations in the Batten Disease Gene, CLN3 von Munroe, Patricia B., Mitchison, Hannah M., O'Rawe, Angela M., Anderson, John W., Boustany, Rose-Mary, Lerner, Terry J., Taschner, Peter E.M., Vos, Nanneke de, Breuning, Martijn H., Gardiner, R. Mark, Mole, Sara E.

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effect of the rpoSam allele on gene expression and stress resistance in Escherichia coli von Galbiati, Heloisa F, Taschner, Natalia P, Spira, Beny

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Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas von van Houtum, W H, Corssmit, E P M, Douwes Dekker, P B, Jansen, J C, van der Mey, A G L, Bröcker-Vriends, A H J T, Taschner, P E M, Losekoot, M, Frölich, M, Stokkel, M P M, Cornelisse, C J, Romijn, J A

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Mutations in the gene–encoding SERCA1, the fast–twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase, are associated with Brody disease von Odermatt, Alex, Taschner, Peter E. M., Khanna, Vijay K., Busch, Herman F. M., Karpati, George, Jablecki, Charles K., Breuning, Martijn H., MacLennan, David H.

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Deletion of the Caenorhabditis elegans homologues of the CLN3 gene, involved in human juvenile neuronal ceroid lipofuscinosis, causes a mild progeric phenotype von Voer, G., Bent, P., Rodrigues, A. J. G., Ommen, G.‐J. B., Peters, D. J. M., Taschner, P. E. M.

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Mutations in the Palmitoyl-Protein Thioesterase Gene (PPT; CLN1) Causing Juvenile Neuronal Ceroid Lipofuscinosis with Granular Osmiophilic Deposits von Mitchison, Hannah M., Hofmann, Sandra L., Becerra, Carlos H. R., Munroe, Patricia B., Lake, Brian D., Crow, Yanick J., Stephenson, John B. P., Williams, Ruth E., Hofman, Irene L., Taschner, Peter E. M., Martin, Jean-Jacques, Philippart, Michel, Andermann, Eva, Andermann, Frederick, Mole, Sara E., Gardiner, R. Mark, O'Rawe, Angela M.

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Characterization of the Gene Encoding Human Sarcolipin (SLN), a Proteolipid Associated with SERCA1: Absence of Structural Mutations in Five Patients with Brody Disease von Odermatt, Alex, Taschner, Peter E.M., Scherer, Stephen W., Beatty, Barbara, Khanna, Vijay K., Cornblath, David R., Chaudhry, Vinay, Yee, Won-Chee, Schrank, Bertold, Karpati, George, Breuning, Martijn H., Knoers, Nine, Maclennan, David H.

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Division behavior and shape changes in isogenic ftsZ, ftsQ, ftsA, pbpB, and ftsE cell division mutants of Escherichia coli during temperature shift experiments von TASCHNER, P. E. M, HULS, P. G, PAS, E, WOLDRINGH, C. L

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Adult neuronal ceroid lipofuscinosis with palmitoyl-protein thioesterase deficiency: First adult-onset patients of a childhood disease von Van Diggelen, Otto P., Thobois, Stephane, Tilikete, Caroline, Zabot, Marie-Thérèse, Keulemans, Joke L. M., Van Bunderen, Patrick A., Taschner, Peter E. M., Losekoot, Monique, Voznyi, Yakov V.

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Polymorphism of μ-opioid receptor gene (OPRM1:c.118a>G) does not protect against opioid-induced respiratory depression despite reduced analgesic response von ROMBERG, Raymonda R, OLOFSEN, Erik, BIJL, Hans, TASCHNER, Peter E. M, TEPPEMA, Luc J, SARTON, Elise Y, VAN KLEEF, Jack W, DAHAN, Albert

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Linkage of Gitelman syndrome to the thiazide-sensitive sodium-chloride cotransporter gene with identification of mutations in Dutch families von LEMMINK, H. H, VAN DEN HEUVEL, L. P. W. J, VAN DIJK, H. A, MERKX, G. F. M, SMILDE, T. J, TASCHNER, P. E. M, MONNENS, L. A. H, HEBERT, S. C, KNOERS, N. V. A. M

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Rapid detection of the major deletion in the Batten disease gene CLN3 by allele specific PCR von Taschner, P E, de Vos, N, Breuning, M H

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Replication of an incomplete alfalfa mosaic virus genome in plants transformed with viral replicase genes von Taschner, Peter E.M., Van Der Kuyl, Antoinette C., Neeleman, Lyda, Bol, John F.

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First-trimester diagnosis of late-infantile neuronal ceroid lipofuscinosis (LINCL) by tripeptidyl peptidase I assay and CLN2 mutation analysis von Kleijer, W. J., van Diggelen, O. P., Keulemans, J. L. M., Losekoot, M., Garritsen, V. H., Stroink, H., Majoor-Krakauer, D., Franken, P. F., Eurlings, M. C. M., Taschner, P. E. M., Los, F. J., Galjaard, R. J. H.

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Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene von Taschner, Peter E.M., Jansen, Jeroen C., Baysal, Bora E., Bosch, Anne, Rosenberg, Efraim H., Bröcker-Vriends, Annette H.J.T., van der Mey, Andel G.L., van Ommen, Gert-Jan B., Cornelisse, Cees J., Devilee, Peter

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Phenotypic dichotomy in mitochondrial complex II genetic disorders von BAYSAL, Bora E, RUBINSTEIN, Wendy S, TASCHNER, Peter E. M

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